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Details
Link-It Detail - Human Phenotype - Abnormal hand morphology
Debug Stats
  • ### Total Build Time: 24 ms 30.977 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 199 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 202 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 3.867 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.084 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 23.037 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal hand morphology HP:0005922
Definition (1)
Any structural anomaly of the `hand` (FMA:9712).
Parents (1)
img Abnormality of the hand HP:0001155
Children (12)
img Narrow palm HP:0004283
img Pointed hand bones HP:0004287
img Minor hand anomalies HP:0003098
img Notched hand bones HP:0004284
img Overmodelled hand bones HP:0004285
img Mitten deformity HP:0004057
img Undermodelled hand bones HP:0004292
img Small hands HP:0200055
img Palmar pits HP:0010610
img Large hands HP:0001176
img Valgus hand deformity HP:0006228
img Hand clenching HP:0001188
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the hand HP:0001155
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the hand HP:0001155
Genes (71)

Species:
human : 71
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUPXQ27.3Q28100874533
img HP IEA, OMIM ID: 300869
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanTET18P100750329Tetrasomy 18p
img HP RolledUp, OMIM ID: 614290
HumanMYMY4100653379Moyamoya disease 4
img HP IEA, OMIM ID: 300845
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanCHMRQ780925Cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
img HP RolledUp, OMIM ID: 610185
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanZDHHC15158866zinc finger, DHHC-type containing 15
img HP RolledUp, OMIM ID: 300577
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
HumanWDR81124997WD repeat domain 81
img HP RolledUp, OMIM ID: 610185
HumanSHANK385358SH3 and multiple ankyrin repeat domains 3
img HP RolledUp, OMIM ID: 606232
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 277590
img HP RolledUp, OMIM ID: 117550
HumanTRPV459341transient receptor potential cation channel, subfamily V, member 4
img HP RolledUp, OMIM ID: 181405
HumanMRXSA57791Armfield X-linked mental retardation syndrome
img HP IEA, OMIM ID: 300261
HumanHDAC855869histone deacetylase 8
img HP RolledUp, OMIM ID: 300882
img HP RolledUp, OMIM ID: 309585
HumanMBD555777methyl-CpG binding domain protein 5
img HP RolledUp, OMIM ID: 156200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0005922Abnormal hand morphology0self